Clinical Research Coordinator, On-Site, Horsham, Pennsylvania
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Job Location:
Hatboro, PA - USA
Monthly Salary:
$ 36600 - 91300
Posted on:
15-09-2025
Vacancies:
1 Vacancy
Job Summary
Join a collaborative patient-centered team where your contributions directly support groundbreaking studies and improved patient outcomes. This is more than just a CRC role its a unique opportunity to deepen your expertise in clinical trial coordination grow within a supportive environment that values professional development and make real progress toward your career goals. Its an ideal fit for a hardworking driven and passionate individual who thrives in a fast-paced team-oriented setting and is eager to make a meaningful impact through clinical research.
Overview:
Coordinate and participate in clinical research studies ensuring that studies are carried out according to protocol contracted scope of work good clinical practice sponsor and Avacare standard operating procedures (SOPs) and any relevant local guidelines and regulations.
Essential Functions
Coordinate clinical research studies conducted by a supervising principle investigator.
May assist as back-up CRC on other studies
Develops and implements patient recruitment strategies; actively recruits to ensure enrollment targets are achieved
Obtains informed consent of research subjects
Develops strong working relationships and maintain effective communication with study team members
Completes all protocol related training
Performs patient/research participant scheduling
Collects patient/research participant history
Collects and maintains source documentation
Manages inventory and administers test articles/investigational productto participants
Performs data entry and query resolution
Supports the collection and review of required essential study documents and reports. Order supportive study supplies (e.g. contracts IXRS lab kits nonclinical supply materials imaging and laboratory handling manuals etc.)
Adheres to an IRB approved protocol
Supports the safety of research subjects report adverse events
Coordinates protocol related research procedures study visits and follow-up
Facilitates pre-study site qualification study initiation monitoring visits and study close out activities
Collects processes and ships laboratory specimens
May be asked to perform special project responsibilities and travel to other clinic locations within the area when needs arise
Complies with Avacare and Sponsor policies standard operating procedures (SOPs) and guidelines
Performs other duties as assigned
Qualifications
Knowledge and ability to apply GCP/ICH and applicable regulatory guidelines
Clinical Research Coordinator experience within a similar setting
Clinical skills experience including obtaining vitals phlebotomy EKG etc.
Knowledge and experienceof site operations and the drug development process
Effective communication
Computer proficiency in use of Microsoft Word Excel
IQVIA is a leading global provider of clinical research services commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race color religion sex sexual orientation gender identity national origin disability status as a protected veteran or any other status protected by applicable law. potential base pay range for this role when annualized is $36600.00 - $91300.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge skills education and experience; location; and/or schedule (full or part-time). Dependent on the position offered incentive plans bonuses and/or other forms of compensation may be offered in addition to a range of health and welfare and/or other benefits.
Required Experience:
IC
Key Skills
- Experience Working With Students
- Google Docs
- Organizational skills
- Classroom Experience
- Data Collection
- Materials Handling
- Workers' Compensation Law
- OSHA
- Special Operations
- Team Management
- Experience with Children
- Supervising Experience
About Company
IQVIA is the Human Data Science Company™. We are inspired by the industry we serve and provide solutions that enable life sciences companies to innovate with confidence, maximize opportunities and ultimately drive human health outcomes forward. Our approach is Human Data Science – a d ... View more
